NDC11 00487020102

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
00487-0201-02	00487-0201
00487-0201-2	00487-0201
00487-201-02	00487-201
0487-0201-02	0487-0201

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ipratropium Bromide and Albuterol Sulfate	IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE	Nephron Pharmaceuticals Corporation	ae35ec1f-526a-49bf-8262-c50e40190d1f	2025-04-08	Warnings, Adverse reactions	Exact identifier ndc (package): 0487-0201-02 ndc (product): 0487-0201 ndc11 (package): 00487020102

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.